Amgen Inc

Amgen Inc(AMGN)資訊與事件

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AMGN 資訊

AMGN 事件

10/20 09:30

AstraZeneca and Amgen's Tezspire Trial Results Show Significant Improvements

Full results from the "positive" Phase 3 CROSSING trial showed that AstraZeneca (AZN) and Amgen's (AMGN) Tezspire demonstrated statistically significant and clinically meaningful improvements in the co-primary endpoints of histologic remission and the frequency and severity of dysphagia in adolescent and adult patients with symptomatic and uncontrolled eosinophilic esophagitis, despite continued treatment with background medications. These improvements were observed at week 24 in both doses tested compared to placebo. Efficacy was sustained in both doses through week 52, as measured in key secondary endpoints. Results from the CROSSING trial were presented in a late-breaking oral presentation at United European Gastroenterology Week 2026 in Barcelona, Spain. Treatment with Tezspire, administered subcutaneously every four weeks, achieved histologic remission for 64.8% for the 210mg dose and 68.9% for the 420mg dose of patients at week 24, compared to 3.5% of patients on placebo. Tezspire also reduced the frequency and severity of dysphagia symptoms by 18.8 points for the 210mg dose and 22.0 points for the 420mg dose from baseline vs. 14.7 points on placebo, as measured by the Dysphagia Symptom Questionnaire score, a patient-reported outcome measure. These results were sustained through week 52, assessed in key secondary endpoints: 67.8% (210mg dose) and 63.3% (420mg dose) of patients taking Tezspire achieved histologic remission vs. 5.4% on placebo and there was continued symptom improvement through week 52, with patients taking Tezspire achieving an average reduction from baseline of 22.1 points (210mg dose) and 24.0 points (420mg dose) in the DSQ score vs. 13.2 points on placebo.

10/20 09:30

AstraZeneca and Amgen's TEZSPIRE Shows Significant Improvement in EoE Symptoms

Full results from the Phase III CROSSING trial showed that AstraZeneca (AZN) and Amgen's (AMGN) TEZSPIRE demonstrated statistically significant and clinically meaningful improvements in the co-primary endpoints of histologic remission and the frequency and severity of dysphagia in adolescent and adult patients with symptomatic and uncontrolled eosinophilic esophagitis, EoE, despite continued treatment with background medications. These improvements were observed at week 24 in both doses tested compared to placebo. Efficacy was sustained in both doses through week 52, as measured in key secondary endpoints.

10/19 08:30

Mattel Appoints Peter Griffith as CFO

Mattel (MAT) announced the appointment of Peter Griffith as Chief Financial Officer, effective October 20, 2026. Griffith succeeds Paul Ruh, who will serve in an advisory role through the end of the year to support an effective transition. Griffith will report to Roger Lynch, Chairman and Chief Executive Officer of Mattel, and will also join the company's board of directors. Most recently, Griffith served as Executive Vice President and CFO of Amgen (AMGN)

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